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solvent for Rick Simpson oil

SkyHighLer

Got me a stone bad Mana
ICMag Donor
Veteran
My easy answer for where to start,

"I. INTRODUCTION

This is the companion document for the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) guidance for industry Q3C Impurities: Residual Solvents (1997), which makes recommendations as to what amounts of residual solvents are considered safe in pharmaceuticals."

http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM073395.pdf

And if you keep pushing G.O. Joe will come up with something like this he tossed out a while back... choose your download, the one I choose has the file identified as, "Urben P.G. (ed.)-Bretherick's Handbook of Reactive Chemical Hazards 2 vols set-AP (2006).pdf"

http://golibgen.io/search.php?search_type=title&search_text=Bretherick&submit=Dig+for

The issue with Hexane is not its toxicity, but that our liver turns it into 2.5 Hexane dione, which is a carcinogen. Long term studies of chronic exposure to hexane by the printing and shoe repair industry, showed significant effects.

Hexane (C6H14) is Class 2, but Pentane (C5H12) is Class 3...

"SOLVENTS GROUPED BY CLASS

Solvents in Class 1 (Table 1) should not be employed in the manufacture of drug substances, excipients, and drug products because of their unacceptable toxicity or their deleterious environmental effect. However, if their use is unavoidable in order to produce a drug product with a significant therapeutic advance, then their levels should be restricted as shown in Table 1, unless otherwise justified. The solvent 1,1,1-Trichloroethane is included in Table 1 because it is an environmental hazard. The stated limit of 1,500 ppm is based on a review of the safety data.

Solvents in Class 2 (Table 2) should be limited in pharmaceutical products because of their inherent toxicity. PDEs are given to the nearest 0.1 mg/day, and concentrations are given to the nearest 10 ppm. The stated values do not reflect the necessary analytical precision of determination. Precision should be determined as part of the validation of the method.

Solvents in Class 3 (Table 3) may be regarded as less toxic and of lower risk to human health. Class 3 includes no solvent known as a human health hazard at levels normally accepted in pharmaceuticals. However, there are no long-term toxicity or carcinogenicity studies for many of the solvents in Class 3. Available data indicate that they are less toxic in acute or short-term studies and negative in genotoxicity studies. It is considered that amounts of these residual solvents of 50 mg per day or less (corresponding to 5,000 ppm or 0.5 percent under Option 1) would be acceptable without justification. Higher amounts may also be acceptable provided they are realistic in relation to manufacturing capability and good manufacturing practice (GMP)."

http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM073395.pdf

Gray Wolf, "At this point, we move to the Greek alphabet with Pentane, which has five carbons and 12 hydrogen’s, to Hexane with six carbons and 12 hydrogen’s, and Heptane with seven carbons. There are longer chain Simple Alkanes, but they are typically not used for extraction.
Due to Vander Waal forces, as the chains get longer, their boiling points go up, as does the difficulty in purging out their residuals afterwards."

https://skunkpharmresearch.com/simple-alkanes-alcohols-and-ethers/

"Laboratory use

Pentanes are relatively inexpensive and are the most volatile liquid alkanes at room temperature, so they are often used in the laboratory as solvents that can be conveniently and rapidly evaporated. However, because of their nonpolarity and lack of functionality, they dissolve only non-polar and alkyl-rich compounds. Pentanes are miscible with most common nonpolar solvents such as chlorocarbons, aromatics, and ethers.

They are often used in liquid chromatography."

"Reactions

Like other alkanes, pentanes are largely unreactive at standard room temperature and conditions - however, with sufficient activation energy (i.e. an open flame), they readily oxidize to form carbon dioxide and water:

C5H12 + 8 O2 → 5 CO2 + 6 H2O + heat/ energy"

https://en.wikipedia.org/wiki/Pentane
 
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SkyHighLer

Got me a stone bad Mana
ICMag Donor
Veteran
Coleman fuel shouldn't be used imo, but I just found guys have been distilling it, and using the lower boiling point fractions, way better... but not for the careless!


dpHarma, 4/16/'99

"Simplicity and effectiveness.

now to distilling highly inflammable solvents.

yep! like the man said. she go boom!

I've sustained probably five or six ether fires over about 10 years.
lucky each time. most were small flashes easily extinguished.
never an explosion.
fires happen rather easily.
explosions are the result of extreme carelessness. If vapours are allowed to build up in a room then contact an ignition source, then well as the man said .....

So how to not go boom? contain the vapours first and foremost. if it don't get into the air, it ain't gonna bother ya none!

Be carefull with spills. try not to.
open flame of any kind is ....... drum roll!~

yes! doh!

cool your receiver flask in ice water even when distilling at atm. pressure.

avoid 'boiling off' solvent into the air unless you have some means of containing it and removing it from the room. ie a fume hood.
so no fume hood, then use your aspirator and shove the output hose down the sink.
attach the vac line to a funnel and position it over your glass pie plate or whatever while driving off the last bit of solvent. The vacuum will suck up all those solvent vapours and carry them down the sewer system. just hope some guy don't toss a match in the crapper. ;-)
or
spring is coming. do it outdoors away from everybody.

peth vapours will catch fire if in contact with a red hot element. ergo, no exposed element. not exposed doesn't mean hidden from view, but enclosed.
but more importantly, there is never a need to have a hot plate so hot.
use a temp controller, and heat only to accomplish distillation.
peth boils starting about 30^C. (not much of THAT in colemans, some brands have more!!) and works on up w/ about 30 to 40% boiling <60^C. after that another 1/3 to ~ 90^C and the rest climbing to say ~110. theres a tiny bit (50 -100mls from 4L) of green colored high boiling lubricant, which will distill if you try. this is what you are leaving behind. also it's a nice idea to separate everything w/ BP <60 and the higher BP which is often referred to as ligroin.
ligroin has greater solvency power and requires higher temps to evaporate.

peth BP 30 - 60^C is ideal for extractions of temp sensitive organics. It will begin to boil from the heat of your hand at atm. pressure.

It's also easy to evaporate completely from your ingestibles.

Peth has an affinty for the cannabinoids.
It doesn't particularly like many organic substances which comprise the biologic makeup of living plants. chlorophyll and flavonoids to mention two.

alcohols solvate most organics and lots of sugars included."

https://the-hive.archive.erowid.org...t=&Number=90292&page=&view=&sort=&part=4&vc=1

Here's a nice presentation of the equipment and process (he's starting with gasoline, but otherwise it's exactly as described above.)

https://youtu.be/YN-U5mepbmk

I'm not encouraging anyone to do this, just an FYI.
 
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